Package 72789-548-93
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
72789-548-93
Digits Only
7278954893
Product NDC
72789-548
Description
180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-548-93)
Marketing
Marketing Status
Brand
metformin hydrochloride
Generic
metformin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47fc43fc-5333-100d-e063-6294a90a5e1b", "openfda": {"upc": ["0372789548937"], "unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["1d0b74de-ef4c-4dd2-8019-2ddb409c60b4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-548-93)", "package_ndc": "72789-548-93", "marketing_start_date": "20260109"}], "brand_name": "Metformin Hydrochloride", "product_id": "72789-548_47fc43fc-5333-100d-e063-6294a90a5e1b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-548", "generic_name": "Metformin Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20271231"}